Weingart, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Weingart, Inc. makes
Weingart, Inc. manufactures ultraviolet sunlamps, including the Model 1000 Sunlamp Product, designed for therapeutic or cosmetic use. The company also produces brownie booths, such as the BB1 model, which incorporate UV lighting for food preparation. Additionally, it supplies electro-sage devices like the Model 203, which use electrical stimulation combined with UV exposure for therapeutic applications.
The company’s products are regulated under FDA’s Class I and Class II categories, with relevant devices listed via the 510(k) pathway. These devices are intended for use in the United States, where compliance with FDA requirements is mandatory. No other regulatory registries or jurisdictions are specified.
Catalogue
Weingart Model 1000 Sunlamp Product Ref K863518
Regimes: 510(k) Registry: 510(k)Brownie Booth BB1 Ref K842975
Regimes: 510(k) Registry: 510(k)Electro-Sage Model 203 Ref K842379
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Weingart, Inc. have in the registry?
The registry currently lists 3 devices for Weingart, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Weingart, Inc.'s devices?
Among its 3 most recently registered devices, Weingart, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Weingart, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Weingart, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Weingart, Inc. in the registry?
The most recently registered devices listed for Weingart, Inc. include WEINGART MODEL 1000 SUNLAMP PRODUCT, BROWNIE BOOTH BB1 and ELECTRO-SAGE MODEL 203.